Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.-Reference-Cited by-同舟云学术

Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.

Published:1994-03-01 Issue:3 Volume:31 Page:213-218
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Jardine P E,Cotter P D,Johnson S A,Fitzsimons E J,Tyfield L,Lunt P W,Bishop D F

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference43 articles.

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4. f-Aminolevulinic acid synthetase activity in erythroblasts of patients with sideroblastic anemia;Takaku, F.; Nakao, K.;Life Sci,1971

5. A case of primary acquired sideroblastic anaemia with deficient f-aminolevulinic acid synthase activity in bone marrow erythroblasts;Tanaka, M.; Ota, H.;Tohoku J Exp Med,1972

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